Good NeighborChildrens Allergy Relief Bubblegum flavor
Good NeighborChildrens Allergy Relief Bubblegum flavor is an FDA drug label for the active ingredient DIPHENHYDRAMINE HCL manufactured by AMERISOURCE BERGEN administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260713.
- Generic name
- DIPHENHYDRAMINE HCL
- Manufacturer
- AMERISOURCE BERGEN
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 46122-793
- Application
- M012
- Label effective
- 20260713
About this product
Good NeighborChildrens Allergy Relief Bubblegum flavor is an FDA-registered drug product whose active ingredient is DIPHENHYDRAMINE HCL. It is labelled by AMERISOURCE BERGEN taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 46122-793, application M012, label effective 20260713. It is one of 90 FDA drug label records sharing the active ingredient DIPHENHYDRAMINE HCL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing DIPHENHYDRAMINE HCL are most often described in connection with: temporarily relieves, symptoms due, hay fever, upper respiratory, allergies runny, nose sneezing, itchy watery, eyes itching. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses ▪ temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ▪ runny nose ▪ sneezing ▪ itchy, watery eyes ▪ itching of the throat or nose
Dosage & Administration
Directions ▪ find right dose on chart below ▪ take every 4 to 6 hours, or as directed by a doctor ▪ do not take more than 6 doses in 24 hours ▪ mL = milliliter Age (yr) Dose (mL) children under 2 years do not use children 2 to 5 years do not use unless directed by a doctor children 6 to 11 years 5 mL to 10 mL Attention: use only enclosed dosing cup designed for use with this product. Do not use any other dosing device.
Warnings
Warnings Do not use ▪ to make a child sleepy ▪ with any other product containing diphenhydramine, even one used on skin Ask a doctor before use if the child has ▪ a breathing problem such as chronic bronchitis ▪ glaucoma Ask a doctor or pharmacist before use if the child is taking sedatives or tranquilizers. When using this product ▪ marked drowsiness may occur ▪ sedatives and tranquilizers may increase drowsiness ▪ excitability may occur, especially in children Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at (1-800-222-1222).
More products with the same ingredient
DIPHENHYDRAMINE HCLAllergy
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View labelAllergy Medicine
View labelAllergy Relief
View labelAllergy Relief
View labelAllergy Relief
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View labelHow products containing DIPHENHYDRAMINE HCL compare
FDA lists 90 drug label records with DIPHENHYDRAMINE HCL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Walgreen Company | 7 |
| — | — | Rite Aid Corporation | 6 |
| — | — | CalmCo LLC | 5 |
| — | — | DOLGENCORP, LLC | 5 |
| — | — | Wal-Mart Stores Inc | 5 |
Recall and safety notices
2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.
| Recall | Product | Firm | Class | Status | Reported |
|---|---|---|---|---|---|
| D-1066-2013 | Ifosfamide Injection 3g/60 mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4496-22 | AmeriSource Bergen | Class II | Terminated | 20131009 |
| D-1065-2013 | Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4495-22 | AmeriSource Bergen | Class II | Terminated | 20131009 |
Frequently asked questions
What is Good NeighborChildrens Allergy Relief Bubblegum flavor used for?
Uses ▪ temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ▪ runny nose ▪ sneezing ▪ itchy, watery eyes ▪ itching of the throat or nose
Who makes Good NeighborChildrens Allergy Relief Bubblegum flavor?
AMERISOURCE BERGEN is the labeler of record for Good NeighborChildrens Allergy Relief Bubblegum flavor. 90 FDA label records share the active ingredient DIPHENHYDRAMINE HCL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Good NeighborChildrens Allergy Relief Bubblegum flavor come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Good NeighborChildrens Allergy Relief Bubblegum flavor prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing DIPHENHYDRAMINE HCL?
Yes. 90 FDA drug label records list DIPHENHYDRAMINE HCL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Good NeighborChildrens Allergy Relief Bubblegum flavor been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.